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Catalysis Communications, ISSN 1566-7367, 01/2014, Volume 43, pp. 173 - 178
Fluoroboric acid (HBF ) adsorbed on mesoporous silica nanoparticles of 25–30 nm dimension was synthesized and characterized by N adsorption, HRTEM, EDX, XPS,... 
Xanthenes | Mesoporous silica nanoparticle | Conjugate Brønsted–Lewis acid | Tetraketones | Conjugate Brønsted-Lewis acid | Conjugate Bronsted-Lewis acid | FLUOROBORIC ACID | CHEMISTRY, PHYSICAL | REUSABLE HETEROGENEOUS CATALYST | EFFICIENT | Nanoparticles | Silica
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2015, Volume 54, Issue 33, pp. 9523 - 9527
A CC bond‐forming conjugate reaction was successfully applied to the enantioselective dearomatization of β‐naphthols. A C(sp2)C(sp3) bond is formed by using... 
naphthols | magnesium | arenes | DFT calculations | aromaticity | OXIDATIVE DEAROMATIZATION | COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | MICHAEL ADDITION | KETONES | PHENOLS | CONSTRUCTION | ESTERS | ALLYLIC DEAROMATIZATION | ALKYNONES | GENERATED MAGNESIUM CATALYST | Models, Molecular | Naphthols - chemistry | Magnesium - chemistry | Stereoisomerism | Ketones - chemistry | Conjugates | Ketones | Asymmetry | Catalysts | Transformations | Magnesium | Ethers | Bonding
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2016, Volume 55, Issue 4, pp. 1460 - 1464
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2017, Volume 56, Issue 14, pp. 4006 - 4010
The enantioselective α‐addition of deconjugated butenolides has rarely been exploited, in contrast to the well‐studied γ‐addition of deconjugated butenolides.... 
butenolides | ortho | dihydrocoumarins | asymmetric catalysis | quinone methides | nucleophilic addition | ortho-quinone methides | ORGANIC-SYNTHESIS | ASYMMETRIC-SYNTHESIS | VINYLOGOUS MICHAEL REACTIONS | NATURAL-PRODUCTS | O-QUINONE METHIDES | CHEMISTRY, MULTIDISCIPLINARY | GAMMA-SUBSTITUTED BUTENOLIDES | ALKYLATING-AGENTS | DIELS-ALDER REACTION | G-QUADRUPLEX | CONJUGATE ADDITION
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 01/2019, Volume 2019, Issue 4, pp. 660 - 664
A C–H alkylation/nucleophilic addition manifold with synthetically useful aryl oximes and pyrazoles was realized by rhodium(III) catalysis under remarkably... 
Domino reactions | Rhodium | C–H functionalization | Homogeneous catalysis | Alkylation | Nucleophilic addition | C-H functionalization | ACTIVATION | IRIDIUM | BOND ALKYLATION | ARYLATION | CHEMISTRY, ORGANIC | CLEAVAGE | CATALYZED HYDROARYLATIONS | FUNCTIONALIZATION | ALKENES | SELECTIVITY | CONJUGATE ADDITION
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2013, Volume 52, Issue 16, pp. 4418 - 4421
Journal Article